Canonical Allele Identifier: CA2580615816
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157201193_157201194del , CM000668.2:g.157201193_157201194del GRCh38
NC_000006.11:g.157522327_157522328del , CM000668.1:g.157522327_157522328del GRCh37
NC_000006.10:g.157564019_157564020del NCBI36
NG_032093.1:g.428264_428265del
NG_032093.2:g.428264_428265del
NG_066624.1:g.430168_430169del

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.4809_4810del ENSP00000055163.8:p.Arg1604ProfsTer?
ENST00000414678.8:c.4878_4879del ENSP00000412835.3:p.Arg1627ProfsTer?
ENST00000637015.2:c.5097_5098del ENSP00000489729.2:p.Arg1700ProfsTer?
ENST00000346085.10:c.4848_4849del ENSP00000344546.5:p.Arg1617ProfsTer?
ENST00000350026.10:c.4560_4561del ENSP00000055163.7:p.Arg1521ProfsTer?
ENST00000414678.7:c.3126_3127del ENSP00000412835.2:p.Arg1043ProfsTer?
ENST00000635849.1:c.2289_2290del ENSP00000490948.1:p.Arg764ProfsTer?
ENST00000635957.1:c.1920_1921del ENSP00000490385.1:p.Arg641ProfsTer?
ENST00000636227.1:n.3431_3432del
ENST00000636254.1:n.888_889del
ENST00000636930.2:c.4968_4969del MANE Select ENSP00000490491.2:p.Arg1657ProfsTer?
ENST00000636940.1:n.2965_2966del
ENST00000637015.1:c.2336_2337del
ENST00000637568.1:c.2250_2251del
ENST00000637741.1:n.1634_1635del
ENST00000637810.1:c.2310_2311del ENSP00000489636.1:p.Arg771ProfsTer?
ENST00000637904.1:c.2469_2470del ENSP00000490550.1:p.Arg824ProfsTer?
ENST00000647938.1:c.4599_4600del ENSP00000498155.1:p.Arg1534ProfsTer?
ENST00000346085.9:c.4599_4600del ENSP00000344546.4:p.Arg1534ProfsTer?
ENST00000350026.9:c.4560_4561del ENSP00000055163.7:p.Arg1521ProfsTer?
ENST00000414678.6:c.3126_3127del ENSP00000412835.2:p.Arg1043ProfsTer?
NM_017519.2:c.4560_4561del NP_059989.2:p.Arg1521ProfsTer?
NM_020732.3:c.4599_4600del NP_065783.3:p.Arg1534ProfsTer?
XM_005267069.3:c.4719_4720del XP_005267126.2:p.Arg1574ProfsTer?
XM_011535984.1:c.3798_3799del XP_011534286.1:p.Arg1267ProfsTer?
XM_011535985.1:c.3618_3619del XP_011534287.1:p.Arg1207ProfsTer?
XM_011535986.1:c.3378_3379del XP_011534288.1:p.Arg1127ProfsTer?
XM_011535987.1:c.2997_2998del XP_011534289.1:p.Arg1000ProfsTer?
XM_011535988.1:c.1860_1861del XP_011534290.1:p.Arg621ProfsTer?
NM_001346813.1:c.4719_4720del NP_001333742.1:p.Arg1574ProfsTer?
NM_001363725.1:c.2469_2470del NP_001350654.1:p.Arg824ProfsTer?
XM_011535984.2:c.4929_4930del XP_011534286.2:p.Arg1644ProfsTer?
XM_011535988.3:c.1860_1861del XP_011534290.1:p.Arg621ProfsTer?
XM_017011103.2:c.4830_4831del XP_016866592.1:p.Arg1611ProfsTer?
XM_017011104.1:c.4800_4801del XP_016866593.1:p.Arg1601ProfsTer?
XM_017011105.2:c.4770_4771del XP_016866594.1:p.Arg1591ProfsTer?
XM_017011106.2:c.4641_4642del XP_016866595.1:p.Arg1548ProfsTer?
XM_017011107.2:c.4620_4621del XP_016866596.1:p.Arg1541ProfsTer?
XR_002956289.1:n.4915_4916del
NM_001363725.2:c.2469_2470del NP_001350654.1:p.Arg824ProfsTer?
NM_001371656.1:c.4848_4849del NP_001358585.1:p.Arg1617ProfsTer?
NM_001374820.1:c.4848_4849del NP_001361749.1:p.Arg1617ProfsTer?
NM_001374828.1:c.4968_4969del MANE Select NP_001361757.1:p.Arg1657ProfsTer?
NM_017519.3:c.4809_4810del NP_059989.3:p.Arg1604ProfsTer?